A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005338



Internal ID7070434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:149315614..149331318hg38UCSC Ensembl
Outerchr7:149012705..149028409hg19UCSC Ensembl
Outerchr7:148643638..148659342hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3815705
hg1915705
hg1815705
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563841
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005338
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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